Prostaglandins and congeners I. The synthesis of 11,15-bisdeoxyprostaglandins E1, E2, and F1α. The stereospecific conjugate addition of a lithium -1-alkenylalanate.-Reference-Cited by-同舟云学术

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Prostaglandins and congeners I. The synthesis of 11,15-bisdeoxyprostaglandins E1, E2, and F1α. The stereospecific conjugate addition of a lithium -1-alkenylalanate.

Published:1972-01 Issue:40 Volume:13 Page:4083-4086
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bernady Karel F.,Weiss Martin J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference4 articles.

1. Total synthesis of (±)-15-deoxyprostaglandin E1

2. A new and convenient method for the preparation of isomerically pure .alpha.,.beta.-unsaturated derivatives via hydroalumination of alkynes

3. Prostaglandins I - total synthesis of 9β,15X-dihydroxyprost-13-enoic acid

4. Stereo-controlled synthesis of dl-prostaglandins F2.alpha. and E2

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2. [(CH2CH)2Al(μ-OCH2CH2NMe2)]2: a vinylalane reagent suitable for conjugate additions to α,β-unsaturated ketones;Tetrahedron Letters;2001-08

3. Lithium Diisobutyl(methyl)aluminum Hydride;Encyclopedia of Reagents for Organic Synthesis;2001-04-15

4. References to Volume 1;Comprehensive Organic Functional Group Transformations;1995

5. One or More CC Bond(s) Formed by Addition;Comprehensive Organic Functional Group Transformations;1995

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